What is NDC 64578-0102?

64578-0102 is the product NDC for Metabopath, Adenosine cyclic phosphate 8 [hp_X]/mL + 30 more ingredients liquid, listed with the FDA by Energetix Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Metabopath (Adenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-Ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, DNA, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, RNA, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum,).

What is the active ingredient?

Adenosine cyclic phosphate, .alpha.-ketoglutaric acid, Adenosine triphosphate disodium, Berberis vulgaris root bark, Anhydrous citric acid, Coenzyme a, Herring sperm DNA, Fumaric acid, Glycyrrhiza glabra, Calcium sulfide, Arctium lappa root, Magnesium phosphate, Dibasic, Manganese acetate tetrahydrate, Nadide, Sodium chloride, Sodium diethyl oxalacetate, Sodium pyruvate, Niacinamide, Pulsatilla vulgaris, Pyridoxine hydrochloride, Frangula purshiana bark, Riboflavin, Saccharomyces cerevisiae RNA, Silicon dioxide, Succinic acid, Sulfur, Thiamine hydrochloride, Thyroid, Bovine, Trifolium pratense flower, Zanthoxylum americanum bark, Zinc gluconate.

Energetix Corporation, NDC labeler code 64578. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Metabopath?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Metabopath NDC 64578-0102 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)64578-0102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width64578-0102Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
64578-0102-1	6457801020164578010201	59.1 mL in 1 BOTTLE, DROPPER (64578-0102-1)Marketed from May 9, 2016

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Metabopath
Generic name (nonproprietary): adenosinum cyclophosphoricum, adenosinum triphosphoricum dinatrum, alpha-ketoglutaricum acidum, berberis vulgaris, citricum acidum, coenzyme a, dna, fumaricum acidum, glycyrrhiza glabra, hepar sulphuris calcareum, lappa major, magnesia phosphorica, manganum aceticum, nadidum, natrum muriaticum, natrum oxalaceticum, natrum pyruvicum, nicotinamidum, pulsatilla, pyridoxinum hydrochloricum, rhamnus purshiana, riboflavinum, rna, silicea, succinicum acidum, sulphur, thiaminum hydrochloricum,
Active ingredients: Adenosine cyclic phosphate — 8 [hp_X]/mL.alpha.-ketoglutaric acid — 12 [hp_X]/mLAdenosine triphosphate disodium — 12 [hp_X]/mLBerberis vulgaris root bark — 4 [hp_X]/mLAnhydrous citric acid — 8 [hp_X]/mLCoenzyme a — 12 [hp_X]/mLHerring sperm DNA — 30 [hp_X]/mLFumaric acid — 12 [hp_X]/mLGlycyrrhiza glabra — 4 [hp_X]/mLCalcium sulfide — 30 [hp_X]/mLArctium lappa root — 4 [hp_X]/mLMagnesium phosphate, Dibasic — 12 [hp_X]/mLManganese acetate tetrahydrate — 10 [hp_X]/mLNadide — 12 [hp_X]/mLSodium chloride — 12 [hp_X]/mLSodium diethyl oxalacetate — 12 [hp_X]/mLSodium pyruvate — 12 [hp_X]/mLNiacinamide — 6 [hp_X]/mLPulsatilla vulgaris — 12 [hp_X]/mLPyridoxine hydrochloride — 6 [hp_X]/mLFrangula purshiana bark — 4 [hp_X]/mLRiboflavin — 10 [hp_X]/mLSaccharomyces cerevisiae RNA — 30 [hp_X]/mLSilicon dioxide — 12 [hp_X]/mLSuccinic acid — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLThiamine hydrochloride — 6 [hp_X]/mLThyroid, Bovine — 9 [hp_X]/mLTrifolium pratense flower — 4 [hp_X]/mLZanthoxylum americanum bark — 4 [hp_X]/mLZinc gluconate — 10 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energetix CorporationNDC labeler code 64578
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 8, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Acidifying Activity (Mechanism)Allergens (Chemical structure)Analogs/Derivatives (Chemical/Ingredient)Calcium Chelating Activity (Mechanism)Cell-mediated Immunity (Physiologic effect)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Copper Ion Absorption (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Magnetic Resonance Contrast Activity (Mechanism)Plant Proteins (Chemical structure)Vitamin B 6 (Chemical/Ingredient)
Identifiers: Product ID 64578-0102_58c9b7a8-1e61-ffc5-e063-6394a90a4ed1SPL ID 58c9b7a8-1e61-ffc5-e063-6394a90a4ed1SPL set ID 58bfe670-d308-45a2-8046-7897b6221452UNII E0399OZS9N, 8ID597Z82X, 5L51B4DR1G, 1TH8Q20J0U, XF417D3PSL, SAA04E81UX, 51FI676N6F, 88XHZ13131, 2788Z9758H, 1MBW07J51Q, 597E9BI3Z3, A1Y870209Z, 9TO51D176N, 0U46U6E8UK, 451W47IQ8X, 6CA025Y4FG, POD38AIF08, 25X51I8RD4, I76KB35JEV, 68Y4CF58BV, 4VBP01X99F, TLM2976OFR, J17GBZ5VGX, ETJ7Z6XBU4, AB6MNQ6J6L, 70FD1KFU70, M572600E5P, MN18OTN73W, 4JS0838828, A4KL1HMZ7T, U6WSN5SQ1Z
Pharmacologic class: Anti-coagulant; Calculi Dissolution Agent; Copper Absorption Inhibitor; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Paramagnetic Contrast Agent; Vitamin B6 Analog

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N464578010201 followed by a unit qualifier and the quantity

Package 64578-0102-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Aug 11, 2026.

Indications (excerpt from the label)

Uses Temporary relief of low energy, food cravings, indigestion.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64578-0102

What is NDC 64578-0102?: 64578-0102 is the product NDC for Metabopath, Adenosine cyclic phosphate 8 [hp_X]/mL + 30 more ingredients liquid, listed with the FDA by Energetix Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Metabopath (Adenosinum Cyclophosphoricum, Adenosinum Triphosphoricum Dinatrum, Alpha-Ketoglutaricum Acidum, Berberis Vulgaris, Citricum Acidum, Coenzyme A, DNA, Fumaricum Acidum, Glycyrrhiza Glabra, Hepar Sulphuris Calcareum, Lappa Major, Magnesia Phosphorica, Manganum Aceticum, Nadidum, Natrum Muriaticum, Natrum Oxalaceticum, Natrum Pyruvicum, Nicotinamidum, Pulsatilla, Pyridoxinum Hydrochloricum, Rhamnus Purshiana, Riboflavinum, RNA, Silicea, Succinicum Acidum, Sulphur, Thiaminum Hydrochloricum,).
What is the active ingredient?: Adenosine cyclic phosphate, .alpha.-ketoglutaric acid, Adenosine triphosphate disodium, Berberis vulgaris root bark, Anhydrous citric acid, Coenzyme a, Herring sperm DNA, Fumaric acid, Glycyrrhiza glabra, Calcium sulfide, Arctium lappa root, Magnesium phosphate, Dibasic, Manganese acetate tetrahydrate, Nadide, Sodium chloride, Sodium diethyl oxalacetate, Sodium pyruvate, Niacinamide, Pulsatilla vulgaris, Pyridoxine hydrochloride, Frangula purshiana bark, Riboflavin, Saccharomyces cerevisiae RNA, Silicon dioxide, Succinic acid, Sulfur, Thiamine hydrochloride, Thyroid, Bovine, Trifolium pratense flower, Zanthoxylum americanum bark, Zinc gluconate.
Who is the labeler?: Energetix Corporation, NDC labeler code 64578. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Metabopath?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.